Primary Device ID | 10845854017920 |
NIH Device Record Key | 8aa8edef-9b5d-4191-b05c-1b0340f519b2 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | C5010A |
Catalog Number | C5010A |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845854017923 [Unit of Use] |
GS1 | 10845854017920 [Package] Contains: 20845854017927 Package: BOX [5 Units] In Commercial Distribution |
GS1 | 20845854017927 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
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